Canonical Allele Identifier: PA2827015300
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50124

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Arg1194Gln
CA020250
NM_001318831.2:c.3581G>A